US3133909A - Monoazo dyestuffs - Google Patents

Monoazo dyestuffs Download PDF

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US3133909A
US3133909A US844638A US84463859A US3133909A US 3133909 A US3133909 A US 3133909A US 844638 A US844638 A US 844638A US 84463859 A US84463859 A US 84463859A US 3133909 A US3133909 A US 3133909A
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acid
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sulfonic acid
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chloride
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Riat Henri
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CIBA Co Inc
CIBA COMPANY Inc
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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
    • C09B62/02—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring
    • C09B62/022—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring the heterocyclic ring being alternatively specified
    • C09B62/026—Azo dyes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
    • C09B62/002—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the linkage of the reactive group being alternatively specified
    • C09B62/006—Azodyes
    • C09B62/012—Metal complex azo dyes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
    • C09B62/02—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring
    • C09B62/04—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring to a triazine ring
    • C09B62/08—Azo dyes
    • C09B62/095—Metal complex azo dyes

Definitions

  • the mobile halogen atom that is to say, the halogen atom capable of reacting with fibrous materials in the presence of an alkali, may be bound in a heterocyclic radical containing two nitrogen atoms, for example, a pyrimidine radical or an acyl radical of an acid containing at least one acid group of the formula ii oH for example, the acyl radical of cyanuric acid or of an aliphatic carboxylic acid.
  • the dyestuffs contain at least one halogen atom bound to a 1:3:5-triazine ring, for example, a dichlorotriazine radical or a monochlorotriazine radical such as the radical of the formula in which Y represents an amino group which may be substituted or a substituted hydroxyl or thio group.
  • the halogenated acyl radicals of aliphatic carboxylic acids advantageously contain few carbon atoms, for example, two or three carbon atoms.
  • dyestuffs of the Formula 1 in which X represents a monochloro-l:315-triazine radical and D represents a benzene or naphthalene radical, and above all complex heavy metal compounds thereof.
  • the radical D may contain further substituents, such as alkoxy, hydroxyl, acylamino, cyano, sulfonyl, sulfamide or nitro groups and/ or halogen atoms.
  • the dyestuffs of this invention can be made from the corresponding amino-monoazo-dyestuifs of the formula in which D has the meaning given above in connection with Formula 1 by methods in themselves known, for example, by acylating them with the anhydride or a halide of an acid of which the acyl radical is capable of reacting with the fibrous material with the formation of a chemical bond.
  • anhydrides or halides of acids having a reactive acyl radical there may be mentioned for example, the anhydrides and halides of aliphatic one-unsaturated carboxylic acids, for example, chloro-maleic anhydride, propionic acid chloride, acrylic acid chloride and especially the halides of aliphatic carboxylic acids containing mobile halogen atoms, such as chloracetyl chloride, sulfochloracetic acid chloride, ,B-bromoor fl-chloro-propionic acid chloride, azfi-dichloropropionic acid chloride, and also trichloropyrimidine (the chloride of barbituric acid) and especially cyanuric chloride or a primary condensation product of cyanurie chloride which contains two chlorine atoms and, instead of the third chlorine atom, a primary amino group or an organic radical.
  • aliphatic one-unsaturated carboxylic acids for example, chloro-maleic anhydride, prop
  • Such primary condensation products of 1 mol of cy-anuric chloride and 1 mol of a reactive organic mercaptoor hydroxyl-compound for example, 1 mol of a phenol or an alcohol
  • a reactive organic mercaptoor hydroxyl-compound for example, 1 mol of a phenol or an alcohol
  • 1 mol of amonia or 1 mol of an organic amine such as methylamine, isopropyl'amine, cyclohexylamine or phenylamine, dimethylamine, ethylamine, ethanolamine, N ethyl phenylamine, y-methoxypropylamine, morpholine, phenylhydrazine sulfonic acid, aminoethane sulfonic acid, aminoacetic acid, ortho-, metaor paraaminobenzoic acid, aminobenzene sulfonic acids, such as phenol sulfonic acids, or ortho-, metaor para-aminobenzene
  • 2:4:6-tribromoor 2:4:6-trichloro-1:3:5-triazine may be reacted, on the one hand, with a dyestuif of the Formula 2 to form a dihalogen-triazine condensation product and, on the other, with amonia or an organic mercaptoor hydroxyl compound or with an organic at most secondary monamine to form a monoh alogen-triazine condensation product.
  • condensations are advantageously carried out with the use of an acid-binding agent, such as sodium carbonate or sodium hydroxide, and under conditions such that one or two exchangeable halogen atoms remain in the final product, that to say, for example, by working in an organic solvent or at a relatively low temperature in an aqueous organic or aqueous medium.
  • an acid-binding agent such as sodium carbonate or sodium hydroxide
  • a diazo-compound especially one of the benzene or naphthalene series, may be coupled in a Weakly acid, neutral or weakly alkaline medium with 1- amino-5-oxyn aphthalene-7-sulfonic acid or a corresponding N-acyl derivative, and, when a l-N-acylamino-S- oxynaphthalene-7-sulfonic acid is used as coupling component, the acyl group is removed after coupling by hydrolysis in a manner in itself known.
  • suitable coupling components there may be mentioned 1amino-5-oxynaphthalene-7-sulfonic acid and its N-acyl derivative.
  • O-acyl derivatives of aminonaphtholsulfonic acids for example, the O-acyl derivatives of l-amino-S-hydroxynaphthalene-3:6- or -4:6-disulfonic acid,
  • Suitable agents yielding metal are, for example, salts containing one of the afore-mentioned metals as the cation, such as chromium sulfates, cobalt acetate, cobalt sulfate, copper sulfate or copper acetate.
  • a complex metal compound for example in the form of a metal-amine complex such as a copperamine sulfate from copper sulfate and ammonia, pyridine or monoethanolamine, or in the form of a compound in which one of the afore-mentioned metals is bound in complex union in the anion, for example a chromium compound of an organic hydroxycarboxylic acid such as salicyclic acid, or a complex cobalt or copper compound of an alkali metal salt of an aliphatic aminocarboxylic or hydroxycarboxylic acid, such as of glycocol, of lactic acid and above all of tartaric acid, such as sodium copper tartrate.
  • a metal-amine complex such as a copperamine sulfate from copper sulfate and ammonia, pyridine or monoethanolamine
  • a complex metal compound for example in the form of a metal-amine complex such as a copperamine sulfate from copper sulfate and ammonia, pyr
  • the treatment with the agent yielding metal may be performed by a method in itself known, for example, at room temperature or at a slightly higher temperature when a readily metallisable parent dyestuff has been used, or, when the metallisation is accompanied by dealkylation, at a temperature ranging from 50 to C. under atmospheric pressure, for example, under refiux, or under superatmospheric pressure, the pH-value depending on the nature of metallisation process used.
  • acid coppering is carried out with copper sulfate, alkaline coppering with copper tetramine sulfate.
  • the metallisation may be carried out in the presence of a solvent, such as alcohol, dimethyl formamide or the like.
  • the resulting metal compound may contain one atom of metal bound in complex union to one or two dyestuff molecules.
  • agent yielding metal there are preferably formed compounds containing one atom of metal for every molecule of dyestuff, and, when chromium or more especially cobalt is used, the 1:2-types are easily formed and especially valuable.
  • Dyestuffs of the invention that contain no heavy metal bound in complex union can alternatively be obtained by a variant of the process described above, wherein a coupling component of the formula in which X represents a halogenated 1:3 S-triazine radical is coupled with a diazotised aromatic amine having sufiicient coupling energy.
  • a coupling component of the formula in which X represents a halogenated 1:3 S-triazine radical is coupled with a diazotised aromatic amine having sufiicient coupling energy.
  • amines are to be understood those which contain no hydroxyl group in the orthoposition relatively to the amino group.
  • the starting compounds of the Formula 3 can be prepared by methods in themselves known by acylating lamino-5-hydroxy-naphthalene-7-sulfonic acid with one of the aforesaid halides or anhydrides.
  • the dyestuffs of the present invention corresponding to the Formula 1 can be isolated and made up into useful dry dyestuif preparations. They are advantageously isolated out at as low a temperature as possible by salting out and filtration.
  • the filtered dyestuif may be dried, if desired, after the addition of an extender and/or buffer, for example, after the addition of a mixture of equal parts of monosodium and disodium phosphate. The drying is advantageously carried out at not too high a temperature and under reduced pressure.
  • the dry preparations of the invention can be made directly, that is to say without intermediate isolation of the dyestuff, by subjecting to spray drying the mixture containing the dyestuff that is obtained in the manufacture of the dyestuff.
  • the dyestuffs of the invention are suitable for dyeing and printing a wide variety of materials, such as silk, leather, wool, superpolyamide fibres, superpolyurethanes, and more especially fibrous cellulosic materials, such as linen, cellulose, regenerated cellulose, and above all cotton. They are especially suitable for dyeing cellulose by the so-called pad dyeing method in which the material is impregnated with an aqueous dyestuff solution, which may contain a salt, and the dyestuif is fixed on the material by an alkaline treatment, preferably at an elevated temperature.
  • This method, and also the directdyeing method which is suitable for many of the dyestuffs of the invention, yield dyeings that are generally distinguished by then good fastness to light and above all by their outstanding properties of wet fastness.
  • the dyeing or print is thoroughly rinsed in warm water and then in cold water, and subjected to a soaping operation, in the presence of an non-ionic dispersing agent and/or wetting agent.
  • EXAMPLE 1 A diazo-compound, prepared in the known manner from 18.9 parts of 2-aminophenol-4-sulfonic acid, is added to a solution, cooled to 5 C., of 26.1 parts of the sodium salt of 1-amino-5-hydroxynaphthalene-7-sulfonic acid, 30 parts of anhydrous sodium carbonate and 30 parts of pyridine in 400 parts of water, and the mixture is stirred until the coupling is complete. The excess of sodium carbonate is neutralised with hydrochloric acid, and the dyestuif is salted out with sodium chloride, filtered off and dried.
  • a solution of 43.9 parts of the dyestuif obtained in this manner in 1000 parts of water is treated with 30 parts of crystalline sodium acetate and then with 100 parts by volume of a molar solution of copper sulfate, and the whole is stirred for 1 hour at 40 to 45 C.
  • the complex copper compound so formed is salted out, if desired, after the addition of a small proportion of acetic acid, filtered off and dissolved in 1000 parts of water.
  • a solution of 18.5 parts of cyanuric chloride in 50 parts of acetone is stirred into a mixture of 200 parts of water and 100 parts of ice.
  • This suspension is treated with an aqueous solution of 19.5 parts of the sodium salt of 1-aminobenzene-3-sulfonic acid, and the liberated acid is neutralized by gradually adding sodium carbonate.
  • the resulting solution of the primary condensation product is mixed with the solution of the copper complex compound prepared as described above, the mixture is heated to 30 to 40 C. and rendered weakly acid to neutral by adding a dilute solution of sodium carbonate. After 3 to 4 hours the monochlorotriazine dyestuft formed is salted out from the solution with sodium chloride, filtered off and dried in vacuo at 80 C.
  • the crude coppering mixture can be used as it is.
  • Dyeing Method 2 parts of the dyestuff is obtained in the above example are dissolved in 100 parts of Wate A cotton fabric is impregnated with this solution until its weight shows an increase of 75%, and then dried.
  • the fabric is then impregnated with a solution at 20 C. containing per liter grams of sodium hydroxide and 300 grams of sodium chloride, squeezed to a weight increase of 75%, steamed for 60 seconds at 100 to 101 C., rinsed, soaped for minutes in a boiling solution of 0.3% strength of a non-ionic detergent, rinsed and dried.
  • a ruby-red dyeing is obtained which is fast to Washing.
  • the dyeing may be carried out as follows:
  • EXAMPLE 2 18.5 parts of cyanuric chloride are dissolved with heating in 60 parts of acetone, and this solution is poured into a mixture of 100 parts of water and 100 parts of ice. The resulting, fine suspension is mixed with the solution of the copper complex compound obtained as described in the first and second paragraphs of Example 1, the mixture is stirred at 0 to 5 C., and the liberated acid is neutralised by the gradual addition of N-sodium hydroxide solution, and 40 parts of ammonia solution of 10% strength are then added. The reaction mixture is heated for 3 hours at 30 to 40 C. The monochlorotriazine dyestuif formed is salted out, filtered off and dried. It dyes cellulose fibers full, pure ruby-red tints.
  • Dyestuffs having similar properties which dye cotton the tints shown in column III of the following table, are obtained by using the copper complexes obtained from the diazo compound of an amine in column I by the process described in one of the preceding examples, by treating said complexes with cyanuric chloride and with an amine shown in column II by the processes described in Examples 1 and 2.
  • EXAMPLE 3 7 whole is refluxed on a boiling Water bath for 4 to 6 hours. 250 parts of sodium chloride are added, the reaction mixture is allowed to cool, and the precipitated copper complex is filtered ofi and then further Worked up as described in Example 1. A dyestuff is obtained which has practically identical properties.
  • EXAMPLE 4 43.9 parts of the dyestuff of the formula (see 1st paragraph of Example 1) are dissolved in 600 parts of water and rendered weakly alkaline with a small amount of sodium carbonate. 120 parts of a solution of sodium chromosalicylate containing 2.6% of chromium are added, the mixture is refluxed at the boil for 4 hours, cooled, and then neutralised with hydrochloric acid.
  • the resulting solution of the 1:2-chromium complex is added to a fine, aqueous, ice-cooled suspension of 19 parts of cyanuric chloride, the mineral acid formed being neutralised with dilute sodium hydroxide solution. After 1 hour 40 parts of ammonia solution of strength are added, and the mixture is allowed to react for 3 hours at 30 to 40 C.
  • the dyestuff formed can be isolated by evaporating the solution in vacuo. It dyes cotton covered grey-violet tints of good fastness to light and very good fastness to wetting.
  • EXAMPLE 5 43.9 parts of the dyestutf of the formula shown in Example 4 are dissolved in 800 parts of water with the addition of 120 parts of N-sodium hydroxide solution, treated with 100 parts of a cobalt sulfate solution containing 3.2% of cobalt, and the whole is heated for 1 hour at 80 C., then cooled, and neutralised with hydrochloric acid.
  • the resulting solution is treated at 0 C. with a solution of 18.5 parts of cyanuric chloride in 60 parts of acetone.
  • the mixture is stirred for 2 hours and constantly kept weakly acid to litmus by continually adding dilute sodium hydroxide solution.
  • 9.5 parts of aniline and 10 parts of sodium bicarbonate are then added, and the mixture is heated to C.
  • EXAMPLE 6 An ice-cooled solution of the copper complex obtained as described in the first and second paragraphs of Example 1 is mixed with a solution of 18.5 parts of cyanuric chloride in 60 parts of acetone, and in the course of 1 hour the reaction mixture is neutralised by gradually adding dilute sodium hydroxide solution. A solution of 9.5 parts of phenol and 4 parts of caustic soda in 100 parts of water is then added, and the mixture is allowed to react for 1 to 2 hours at room temperature. The dyestufi is then salted out, filtered off and dried. It dyes cotton ruby-red tints.
  • a dyestutr having similar properties is obtained when 11.1 parts of thiophenol instead of 9.5 parts of phenol are used.
  • the 9.5 parts of phenol may also be replaced by 19.6 parts of the sodium salt of phenol-3-sulfonic acid or of phenol-4-sulfonic acid.
  • the dyestuffs formed can in this case be obtained by treating the reaction mixture with equal parts of monosodium and disodium phosphate and evaporating it to dryness in vacuo. These dyestuffs produce on cotton ruby-red tints having very good properties of fastness.
  • EXAMPLE 7 The procedure is the same as that used in Example 1, except that the primary condensation product from cyanuric chloride and methanilic acid is replaced by a solution of 18 parts of 6-'nethoxy-2:4-dichlorotriazine in parts of acetone. A dyestuff is obtained which dyes cotton fast ruby-red tints.
  • EXAMPLE 8 50 parts of the copper complex of the formula O-Cu0 are dissolved in 1200 parts of water. The solution is rendered neutral and treated portionwise at room temperature with 15 parts of fi-chloropropionyl chloride, and the mineral acid formed is gradually neutralised with a dilute sodium hydroxide solution, or by strewing in solid sodium bicarbonate. On completion of the reaction the dyestuff is salted out, filtered ofi and dried. It dyes cotton fast ruby-red tints.
  • Dyestuffs having similar properties are obtained when the B-chloropropionyl chloride is replaced by an appropriate proportion of uzfi-dichloropropionyl chloride or acrylyl chloride or azB-dibromopropionyl chloride or acrylic anhydride or chloromaleic anhydride.
  • EXAMPLE 9 A solution of 50 parts of the copper complex mentioned in Example 8 in 1000 parts of water is neutralised with sodium carbonate. 25 parts of crystalline sodium acetate and a solution of 20 parts of 2:4:6-trichloropyrimidine in 200 parts of alcohol are then added, and the mixture is vigorously stirred for 4 hours at 50 to 60 C. The dyestufr formed is salted out, filtered off and dried. It dyes cotton ruby-red tints. The analysis of the dyestufi reveals that it contains 1.9 atoms of chlorine for every azo group.
  • EXAMPLE 10 40.4 parts of the dyestuff obtained from diazotised 4- nitro-Z-aminophenol and 1-amino-5-hydroxynaphthalene- 7-sulfonic acid in a solution rendered alkaline with sodium carbonate, in the presence of pyridine bases, are converted into the corresponding chromium complex as described in Example 4. This complex is salted out with sodium chloride, filtered off, again dissolved in 1000 parts of water containing 10 parts of sodium bicarbonate, and mixed at 30 to 40 C. with a neutralized solution of the primary condensation product from 19 parts of cyanuric chloride and 17.3 parts of 1-aminobenzene-3- sulfonic acid. On completion of the reaction the dyestuff is salted out and filtered off. It dyes cotton fast reddish black-grey tints.
  • a greenish blue-gray dyestufi having similar properties is obtained by replacing the above 4-nitro-2-aminophenol by the corresponding 5-nitro-compound.
  • EXAMPLE 11 A solution of 26.1 parts of the sodium salt of 1- amino-S-hydroxy-naphthalene-7-sultonic acid in 400 parts of water is mixed with an aqueous solution of 34.2 parts of the sodium salt of 6-(3-sulfophenyl)-amino-2:4-dichlorotriazine, and the mixture is heated to 25 to 30 C. In the course of 2 to 3 hours a dilute solution of sodium hydroxide is added dropwise in a manner such that the pH value of the reaction mixture remains constant at 5.5 to 6.6.
  • the resulting solution of the monochlorotriazine compound is cooled to to C. and mixed with 20 parts of sodium bicarbonate.
  • the diazo compound obtained in the usual manner from 17.3 parts of l-aminobenzene- 3-sulfonic acid is then run in.
  • the dyestuff formed in this manner dyes cellulose fibers red-orange tints which are very fast to Washing.
  • dyestuffs are obtained which yield slightly more yellowish or reddish tints respectively.
  • 1-amino-4-methoxybenzene- 2-sulfonic acid dyes red tints, as does Z-aminonaphthalene-4z8-disulfonic acid.
  • the triazine compound used in the above example can be replaced by an equal amount of 6-(4'-sulfophenyl)- amino-2:4-dichlorotriazine, to yield dyestuffs having very similar properties.
  • the dyestuif used in this example can be prepared by coupling the diazo compound of 1-aminobenzene-3-sulfom'c acid in a solution alkalinised with sodium carbonate with 1-amino-5-hydroxynaphthalene-7- sulfonic acid, and treating the resulting dyestufi with the triazine derivative.

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US844638A 1958-10-13 1959-10-06 Monoazo dyestuffs Expired - Lifetime US3133909A (en)

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CH6498458A CH370504A (de) 1958-10-13 1958-10-13 Verfahren zur Herstellung neuer Monoazofarbstoffe

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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3225027A (en) * 1962-01-29 1965-12-21 Ici Ltd Reactive naphthol monoazo dyestuffs
US3227705A (en) * 1962-01-30 1966-01-04 Ici Ltd Copper containing disazo dyestuffs
US3354140A (en) * 1959-04-10 1967-11-21 Sandoz Ltd Metal-containing reactive monoazo dyestuffs containing a triazine group
US3502642A (en) * 1967-07-24 1970-03-24 Geigy Ag J R Reactive copper-containing benzeneazonaphthalene dyes containing a trichloropyrimidine group
US4126609A (en) * 1972-07-03 1978-11-21 Bayer Aktiengesellschaft Azo dyestuff with a fiber-reactive group attached to a naphthalene sulphonic acid component
US4145340A (en) * 1973-01-30 1979-03-20 Imperial Chemical Industries Limited Water-soluble reactive monoazo dye containing a nonylphenoxy, chlorotriazine group
US5106958A (en) * 1985-11-21 1992-04-21 Sandoz Ltd. 1:1 copper complexes of further unsubstituted or substituted 6-(2'-chloro-4'-substituted amino-1,3,5- triazin-6'-ylamino)-1-hydroxy-2-(2'-hydroxy-5'-sulfophenylazo)-3- sulfonaphthalenes

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US654064A (en) * 1900-04-03 1900-07-17 Basf Ag Blue monoazo dye.
US1886480A (en) * 1929-04-11 1932-11-08 Chem Ind Basel Dyestuffs containing cellulose residues and process of making same
US2041851A (en) * 1932-07-07 1936-05-26 Ici Ltd Azo dyestuffs and their production
US2873269A (en) * 1956-09-14 1959-02-10 Ciba Ltd Monoazo-dyestuffs
US2892671A (en) * 1959-06-30 Coloring process

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2892671A (en) * 1959-06-30 Coloring process
US654064A (en) * 1900-04-03 1900-07-17 Basf Ag Blue monoazo dye.
US1886480A (en) * 1929-04-11 1932-11-08 Chem Ind Basel Dyestuffs containing cellulose residues and process of making same
US2041851A (en) * 1932-07-07 1936-05-26 Ici Ltd Azo dyestuffs and their production
US2873269A (en) * 1956-09-14 1959-02-10 Ciba Ltd Monoazo-dyestuffs

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3354140A (en) * 1959-04-10 1967-11-21 Sandoz Ltd Metal-containing reactive monoazo dyestuffs containing a triazine group
US3225027A (en) * 1962-01-29 1965-12-21 Ici Ltd Reactive naphthol monoazo dyestuffs
US3227705A (en) * 1962-01-30 1966-01-04 Ici Ltd Copper containing disazo dyestuffs
US3502642A (en) * 1967-07-24 1970-03-24 Geigy Ag J R Reactive copper-containing benzeneazonaphthalene dyes containing a trichloropyrimidine group
US4126609A (en) * 1972-07-03 1978-11-21 Bayer Aktiengesellschaft Azo dyestuff with a fiber-reactive group attached to a naphthalene sulphonic acid component
US4145340A (en) * 1973-01-30 1979-03-20 Imperial Chemical Industries Limited Water-soluble reactive monoazo dye containing a nonylphenoxy, chlorotriazine group
US5106958A (en) * 1985-11-21 1992-04-21 Sandoz Ltd. 1:1 copper complexes of further unsubstituted or substituted 6-(2'-chloro-4'-substituted amino-1,3,5- triazin-6'-ylamino)-1-hydroxy-2-(2'-hydroxy-5'-sulfophenylazo)-3- sulfonaphthalenes

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BE583502A (fr) 1960-04-12

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